AI Article Synopsis

  • The study assessed the probiotic potential and safety of seven Enterococcus faecalis strains from healthy Chinese infants, focusing on various survival and adhesion factors.
  • All strains showed good tolerance to low pH, NaCl, and bile salts, with strain A3-1 demonstrating superior adhesion, antibacterial activity, and biofilm production.
  • While the isolates carried several virulence genes, none displayed significant pathogenic traits and showed varying susceptibility to antibiotics, with strain A3-1 identified as the most promising probiotic candidate.

Article Abstract

The aim of this study was to evaluate the probiotic characteristics and safety of seven Enterococcus faecalis isolates from fecal samples of healthy Chinese infants. We evaluated the isolates' tolerance to low pH, survival in bile salts and NaCl, adhesion ability, biofilm formation, antimicrobial activity, toxin gene distribution, hemolysis, gelatinase activity, antibiotic resistance, and virulence to Galleria mellonella. All strains survived at pH 5.0, in 7.0% NaCl, and in 3% bile salt. Adhesion to Caco-2 cells was above 10%. Strain A3-1 had higher adhesion ability toward mucin, collagen, and BSA in vitro, better antibacterial activity, and the strongest biofilm production. We detected seven virulence genes with a distribution of asa1 (100%), cylA (71.4%), esp (85.7%), hyl (14.3%), gelE (85.7%), ace (42.9%), and agg (71.4%). Although all strains were γ-hemolytic, none showed gelatinase activity based on physiological activity detection. All isolates were susceptible to benzylpenicillin, ampicillin, ciprofloxacin, levofloxacin, moxifloxacin, tigecycline, nitrofurantoin, linezolid, and vancomycin; they were not susceptible to erythromycin, quinupristin/dalofopine, and clindamycin. The virulence test of G. mellonella showed that, except for strains 106-1 and 113-1, the other strains had toxicity lower than 10%. Strain A3-1 may have the greatest potential to be developed as a probiotic.

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http://dx.doi.org/10.1007/s12602-019-09625-7DOI Listing

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